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Merck
CN

526037

Cyclopentanecarboxaldehyde

95%

Synonym(s):

Cyclopentanealdehyde, Cyclopentanecarbaldehyde, Cyclopentyl aldehyde, Cyclopentylformaldehyde, Formylcyclopentane

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About This Item

Linear Formula:
C5H9CHO
CAS Number:
Molecular Weight:
98.14
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
95%
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Quality Level

assay

95%

contains

0.1% hydroquinone as stabilizer

refractive index

n20/D 1.4430 (lit.)

bp

140-141 °C (lit.)

density

0.919 g/mL at 25 °C (lit.)

functional group

aldehyde

storage temp.

2-8°C

SMILES string

[H]C(=O)C1CCCC1

InChI

1S/C6H10O/c7-5-6-3-1-2-4-6/h5-6H,1-4H2

InChI key

VELDYOPRLMJFIK-UHFFFAOYSA-N

General description

Cyclopentanecarboxaldehyde can be prepared from cyclohexene, via copper-catalyzed oxidation with persulfate. It can also be synthesized from mercuric sulfate and cyclohexene.

Application

Cyclopentanecarboxaldehyde may be used in the synthesis of:
  • D,L-trans-2-cyclopentylmethylene-1-nitroso-1-(2-hydroxycyclohexyl)hydrazine
  • ethyl 5-cyclopentyl-5-hydroxy-2-pentenoate
  • ethyl 3-cyclo entyl-3-hydroxy-2-vinylpropanoate


pictograms

FlameExclamation mark

signalword

Warning

Hazard Classifications

Aquatic Chronic 3 - Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

3 - Flammable liquids

wgk

WGK 3

flash_point_f

82.9 °F - closed cup

flash_point_c

28.3 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

Regulatory Information

危险化学品

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Mechanism of oxidation of the 2-hydroxycyclohexyl radical to cyclopentanecarbaldehyde by copper ions in aqueous solutions.
Masarwa M, et al.
Inorganic Chemistry, 30(8), 1849-1854 (1991)
Cyclopentanecarboxaldehyde.
Grummitt O, et al.
Organic Syntheses, 26-26 null
2-Hydroxycyclohexylhydrazines. II. 1 Reaction with Nitrous Acid.
Taguchi T, et al.
The Journal of Organic Chemistry, 29(5), 1104-1106 (1964)



Global Trade Item Number

SKUGTIN
526037-5G04061832552330
526037-1G04061832552323